Canonical Allele Identifier: PA2741842164
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504335
ClinVar RCV Id: RCV003231796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Thr1475Ile
CA388894152
NM_001170629.2:c.4424C>T